Have questions? Visit https://www.reddit.com/r/SNPedia

rs606231390

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs606231390(-;-)
Make rs606231390(-;A)
Make rs606231390(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position43092839
GeneBRCA1
is asnp
is mentioned by
dbSNPrs606231390
ebirs606231390
HLIrs606231390
Exacrs606231390
Varsomers606231390
Maprs606231390
PheGenIrs606231390
hapmaprs606231390
1000 genomesrs606231390
hgdprs606231390
ensemblrs606231390
gopubmedrs606231390
geneviewrs606231390
scholarrs606231390
googlers606231390
pharmgkbrs606231390
gwascentralrs606231390
openSNPrs606231390
23andMers606231390
23andMe allrs606231390
SNP Nexus

SNPshotrs606231390
SNPdbers606231390
MSV3drs606231390
GWAS Ctlgrs606231390
Max Magnitude0
ClinVar
Risk rs606231390(A;A)
Alt rs606231390(A;A)
Reference Rs606231390(;)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41244854dupT
CLNSRC Breast Cancer Information Core (BRCA1)
CLNACC RCV000047935.2, RCV000111919.3,